Water → 5-Methylisoquinoline

HRID 343318Notes

Reaction equation

HRID 343318 reaction equation
C[Mg]I.Br[C:5]1[CH:14]=[CH:13][CH:12]=[C:11]2[C:6]=1[CH:7]=[CH:8][N:9]=[CH:10]2.O.[CH3:16]C(OCC)=O>CCOCC.Cl[Ni]1(Cl)[P](C2C=CC=CC=2)(C2C=CC=CC=2)CCC[P]1(C1C=CC=CC=1)C1C=CC=CC=1>[CH3:16][C:5]1[CH:14]=[CH:13][CH:12]=[C:11]2[C:6]=1[CH:7]=[CH:8][N:9]=[CH:10]2

Participants

7

Procedure

A 3M solution of methyl magnesium iodide in ether (50 ml, 0.15 mol) was added dropwise to a stirred, ice-cooled solution of 5-bromoisoquinoline (21 g, 0.10 mol), obtained by the method described in J. Org. Chem., 1964, 29, 329, and [1,3-bis(diphenylphosphino)-propane]nickel(II) chloride (400 mg, 0.7 mmol) in anhydrous ether and the reaction mixture heated under reflux for 5 days, allowed to cool, then poured into water (500 ml). The organic phase was separated, combined with ether extracts of the aqueous phase, washed with saturated brine, dried (MgSO4) and evaporated under reduced pressure to yield an oil, chromatography of which on silica gel, using a 5-50% ether in hexane elution gradient, provided the required. product (8.4 g). Rf 0.40 (SS 8), m/e 144 (M+H)+. Found: C,79.57; H,6.26; N,8.61. C10H9N; 0.27 CH3CO2CH2CH3 requires C,79.70; H,6.74; N,8.39%.

Workup

  1. customobtained by the method
  2. temperatureunder reflux for 5 days
  3. temperatureto cool
  4. customThe organic phase was separated
  5. washwashed with saturated brine
  6. dry with materialdried (MgSO4)
  7. customevaporated under reduced pressure
  8. customto yield an oil, chromatography of which on silica gel
  9. washa 5-50% ether in hexane elution gradient
  10. customprovided the

Sources & evidence

ORD record
ord-5ac241919a4d4f87b01e0fc7deca7e50
Source dataset
uspto-grants-1999_01
Patent number
US05861393

Reaction notes

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